和男人发生性关系的男人
失调
混淆
肠道菌群
医学
免疫学
毛螺菌科
微生物群
人类免疫缺陷病毒(HIV)
生理学
生物
内科学
生物信息学
厚壁菌
细菌
梅毒
遗传学
16S核糖体RNA
作者
Ivan Vujkovic-Cvijin,Ornella Sortino,Eveline Verheij,Jack Sklar,Ferdinand W.N.M. Wit,Neeltje A. Kootstra,Brian A. Sellers,Jason M. Brenchley,Jintanat Ananworanich,Maarten Schim van der Loeff,Yasmine Belkaid,Peter Reiss,Irini Sereti
标识
DOI:10.1038/s41467-020-16222-8
摘要
Abstract Loss of gut mucosal integrity and an aberrant gut microbiota are proposed mechanisms contributing to chronic inflammation and increased morbidity and mortality during antiretroviral-treated HIV disease. Sexual practice has recently been uncovered as a major source of microbiota variation, potentially confounding prior observations of gut microbiota alterations among persons with HIV (PWH). To overcome this and other confounding factors, we examine a well-powered subset of AGEhIV Cohort participants comprising antiretroviral-treated PWH and seronegative controls matched for age, body-mass index, sex, and sexual practice. We report significant gut microbiota differences in PWH regardless of sex and sexual practice including Gammaproteobacteria enrichment, Lachnospiraceae and Ruminococcaceae depletion, and decreased alpha diversity. Men who have sex with men (MSM) exhibit a distinct microbiota signature characterized by Prevotella enrichment and increased alpha diversity, which is linked with receptive anal intercourse in both males and females. Finally, the HIV-associated microbiota signature correlates with inflammatory markers including suPAR, nadir CD4 count, and prevalence of age-associated noncommunicable comorbidities.
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